Perfluoropyridine as a Scaffold for Semifluorinated Thiol‐ene Networks with Readily Tunable Thermal Properties

Two new trifunctional alkene monomers based on the highly modular perfluoropyridine scaffold are synthesized with an aliphatic and an aromatic moiety, 4‐penten‐1‐ol and eugenol, respectively. The monomers are the basis for thiol‐ene thermoset materials, formulated against a difunctional or trifuncti...

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Veröffentlicht in:Macromolecular chemistry and physics 2020-06, Vol.221 (12), p.n/a, Article 2000100
Hauptverfasser: Moore, Levi M. J., Greeson, Kevin T., Stewart, Kevin A., Kure, Daniel A., Corley, Cynthia A., Jennings, Abby R., Iacono, Scott T., Ghiassi, Kamran B.
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Sprache:eng
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Zusammenfassung:Two new trifunctional alkene monomers based on the highly modular perfluoropyridine scaffold are synthesized with an aliphatic and an aromatic moiety, 4‐penten‐1‐ol and eugenol, respectively. The monomers are the basis for thiol‐ene thermoset materials, formulated against a difunctional or trifunctional thiol. Systems based on these novel monomers have a wide range of thermal properties, with glass transition temperatures (Tgs) spanning from −42 to 21 °C. Mixed systems obey the Fox equation, and Tgs of the mixtures can be tuned to specific values in that range. Thermal degradation temperatures follow a similar trend, with decomposition temperatures ranging from 274 to 348 °C in nitrogen with varying compositions having tailorability therein. This new class of semifluorinated thermoset materials with tunable thermal properties has several potential applications within the aerospace industry, such as sealants and coatings, where stability and survivability at high temperatures in harsh environmental conditions are imperative. Two new trifunctional alkene monomers based on the highly modular perfluoropyridine scaffold are synthesized in high yield at scalable quantities using an alipahtic or aromatic alcohol. Thermoset thiol‐ene systems from these materials show readily tunable thermal properties (Tg, degradation temperature) based on the identity of the alkene moiety, polythiol comonomer, and formulations thereof.
ISSN:1022-1352
1521-3935
DOI:10.1002/macp.202000100